ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.7714A>G (p.Ile2572Val)

dbSNP: rs1555452734
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000517829 SCV000614533 uncertain significance not specified 2016-10-24 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005010473 SCV005638289 uncertain significance Polycystic kidney disease, adult type 2024-01-14 criteria provided, single submitter clinical testing

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